首页> 美国卫生研究院文献>Infection and Immunity >Phosphatidylinositol-specific phospholipase C from Listeria monocytogenes contributes to intracellular survival and growth of Listeria innocua.
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Phosphatidylinositol-specific phospholipase C from Listeria monocytogenes contributes to intracellular survival and growth of Listeria innocua.

机译:单核细胞增生利斯特氏菌的磷脂酰肌醇特异性磷脂酶C有助于无毒李斯特菌的细胞内存活和生长。

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摘要

Listeria monocytogenes is a facultative intracellular organism that is capable of replicating within macrophage and macrophage-like cells. The species secretes a phosphatidylinositol-specific phospholipase C (PI-PLC) encoded by the plcA gene. A plcA gene from L. monocytogenes was cloned downstream of a gram-positive promoter in the plasmid pWS2-2. To determine what effect plcA would have on intracellular survival when introduced into Listeria innocua, a species that does not growth intracellularly or contain plcA, transformation with the recombinant pWS2-2 plasmid was performed. Phospholipase C activity in Listeria innocua/pWS2-2 was confirmed on a brain heart infusion-phosphatidylinositol agar plate, whereas wild-type L. innocua did not produce PI-PLC activity. Intracellular growth of L. innocua/pWS2-2 was subsequently measured in the macrophage-like cell line J774 by Giemsa staining and viable count determinations at specific time points following infection. The J774 cells infected with wild-type L. innocua showed a falling viable count through 8 h postinfection. Although J774 cells infected with L. innocua/pWS2-2 also initially displayed reduced viable counts, the viable count rose after 6 h postinfection and increased further at 8 h postinfection before a subsequent decline again at 16 h postinfection. Giemsa staining revealed fewer than 6 bacteria in individual macrophage cells at 2 h postinfection, and yet approximately 15% of the J774 cells had 6 to 12 bacteria localized to one area of the macrophage cell after 6 h; moreover, electron micrographs showed that the L. innocua/pWS2-2 cells were replicating inside the phagosome of the host cell. Furthermore, Thoria Sol labeling demonstrated that lysosomes had fused with these phagosomes, and acridine orange staining revealed that the compartments were acidified. These results demonstrate that L. innocua cells transformed with the plasmid-borne plcA gene, and expressing functional PI-PLC, are able to grow intracellularly in what appear to be phagolysosomes, although between 3 and 6 h is needed for this to manifest itself. Intracellular growth specifically in L. innocua may be a secondary function associated with the plcA gene product. The addition of this one gene, plcA, to a species of Listeria that in the wild-type state does not replicate intracellularly apparently can now allow some of the bacteria to transiently multiply inside the phagosomes of host macrophage cells.
机译:单核细胞增生李斯特菌是兼性的细胞内生物,能够在巨噬细胞和巨噬细胞样细胞内复制。该物种分泌由plcA基因编码的磷脂酰肌醇特异性磷脂酶C(PI-PLC)。将来自单核细胞增生李斯特氏菌的plcA基因克隆到质粒pWS2-2中革兰氏阳性启动子的下游。为了确定将plcA引入无菌李斯特菌(一种不在细胞内生长或不包含plcA的物种)后对细胞内存活的影响,进行了重组pWS2-2质粒的转化。在脑心脏输注磷脂酰肌醇琼脂平板上证实了无病李斯特菌/ pWS2-2中的磷脂酶C活性,而野生型无病李斯特菌不产生PI-PLC活性。随后在感染后的特定时间通过吉姆萨(Giemsa)染色和活计数测定在巨噬细胞样细胞系J774中测量了无毒李斯特菌/ pWS2-2的细胞内生长。感染野生型无毒利什曼原虫的J774细胞在感染后8小时内的存活计数下降。尽管感染了无毒李斯特菌/ pWS2-2的J774细胞最初也显示出减少的活菌计数,但活菌计数在感染后6 h后上升,并在感染后8 h进一步上升,然后在感染后16 h再下降。 Giemsa染色显示,感染后2 h,单个巨噬细胞中的细菌少于6个,而6小时后,约15%的J774细胞中有6至12个细菌位于巨噬细胞的一个区域。此外,电子显微照片显示,无毒乳杆菌/ pWS2-2细胞在宿主细胞的吞噬体内复制。此外,Thoria Sol标记显示溶酶体已与这些吞噬体融合,and啶橙染色表明隔室已被酸化。这些结果表明,用质粒携带的plcA基因转化并表达功能性PI-PLC的无毒李斯特菌细胞能够在细胞内生长,似乎是吞噬体,尽管这需要3至6小时才能显现出来。具体而言,在无毒乳杆菌中的细胞内生长可能是与plcA基因产物相关的第二功能。现在,将这种基因plcA添加到在野生型状态下不会明显在细胞内复制的利斯特氏菌物种中,现在可以使某些细菌在宿主巨噬细胞的吞噬体内瞬时繁殖。

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